Propecia

   
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Propecia


Drug - Propecia
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Finasteride
Multiple ingredients are in alphabetical order.

Strength - 1MG
The potency of the active ingredient(s), Finasteride. May repeat for multiple part products.

Applicant - MERCK
The firm name holding legal responsibility for Propecia. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020788
The FDA assigned number to Propecia. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Propecia. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Dec 19, 1997
The date Propecia was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".

Reference Listed Drug (RLD) - Yes
The pioneer or innovator of Propecia. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - RX
The group or category of approved drugs Propecia is in. Format is RX, OTC, DISCN.

Applicant Full Name - Merck Research Laboratories Div Merck Co Inc
The full name of the firm holding legal responsibility for the new application of Propecia.

Propecia